“Trial Master File” jobs in Canada – Page 3

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• 1mo

  Clinical Research Associate - Canada

  Remote in Canada

  RemoteFull Time

  

  Syneos Health, LLC

  Candidates need a bachelor's degree or RN in a related field, or equivalent experience. They need knowledge of GCP/ICH guidelines, good computer skills, strong communication skills and the ability to travel up to 75%.

  Electronic data capture systems, Trial Master File, Clinical data tracking systems

  1mo

  Clinical Trial Manager - Full Service

  Remote in Canada

  RemoteFull Time

  

  Syneos Health, LLC

  Candidates need a bachelor's degree or RN in a related field, proven leadership of teams and project milestones, and expertise in site management and monitoring. They also need knowledge of GCP/ICH guidelines, budget management, conflict resolution and good computer skills, and preferably experience with risk-based monitoring.

  CTMS, Electronic Data Capture (EDC), Trial Master File (TMF), eDiary, ePRO, IVRS/IWRS

  1mo

  Clinical Research Associate - Sponsor Dedicated - Bilingual (French/English) Homebased- Quebec,Canada

  Remote in Canada

  RemoteFull Time

  

  Syneos Health, LLC

  Candidates need fluency in both French and English, plus clinical monitoring experience and a working knowledge of ICH-GCP, relevant regulations and company SOPs. Strong judgment, adaptability to changing priorities and comfort with electronic data capture systems are expected.

  Electronic data capture systems, Tracking systems, Case report forms

  1mo

  Sr CTM

  Remote in Canada

  RemoteFull Time

  

  Syneos Health, LLC

  Syneos Health needs candidates with a bachelor's degree or RN in a related field, demonstrated site management and monitoring expertise, and knowledge of GCP and ICH guidelines. Strong leadership, conflict resolution, budget and computer skills are also required.

  CTMS, EDC, eDiary, ePROs, Trial Master File (TMF), IVRS/IWRS

  1mo

  Experienced Clinical Research Associate - Sponsor Dedicated

  Remote in Canada

  RemoteFull Time

  

  Syneos Health, LLC

  Candidates need a bachelor's degree or RN in a related field, knowledge of Good Clinical Practice and ICH guidelines, good computer skills, and strong communication skills. Travel of up to 75% on a regular basis is required.

  Electronic data capture systems, Tracking systems

• 1mo

  Sr Project Manager - Full Service

  Remote in Canada

  RemoteFull Time

  SH

  Syneos Health Canada LP

  Candidates need a Bachelor's degree in a life sciences or health discipline, CRO experience and proven experience independently managing clinical trials. They also need strong knowledge of GCP, ICH guidelines and clinical development, plus strong communication and leadership skills.

  Leadership, Clinical research, Clinical trials, Google Cloud, Customer service, Stakeholder management

  1mo

  Site Activation Specialist II Remote in Canada-QC-Montreal (Client Dedicated)

  Montréal, QC

  RemoteFull Time

  SH

  Syneos Health Canada LP

  Syneos Health Canada LP needs a bachelor's degree, detailed knowledge of clinical trial processes across Phases II to IV and ICH GCP, and clinical trial start-up experience. Candidates must be fluent in French and English and able to negotiate, manage vendors and handle multiple budgets.

  Regulatory compliance, Process improvement, Communication skills, SAM, Data protection, Quality control

• 1mo

  Clinical Research Manager- FSP

  Quebec

  Remote

  PI

  Parexel International (Canada) LTD

  5+ YOECandidates need five to six years of clinical research experience, ideally as a CRA, with strong project management and clinical trial knowledge. A bachelor's degree in science is required, and an advanced degree is preferred.

  CTMS, eTMF

  1mo

  Clinical Trial Coordinator- Finance- FSP

  Quebec

  Remote

  PI

  Parexel International (Canada) LTD

  1+ YOEParexel needs candidates with one to two years in clinical research or healthcare, a life sciences or equivalent background, and budget negotiation experience. Candidates should know Good Clinical Practice and Good Documentation Practice, and be strong in Microsoft Excel and fluent in English and French.

  CTMS, eTMF

  1mo

  Global Site Start Up Lead - FSP

  Ontario

  Remote

  PI

  Parexel International (Canada) LTD

  4+ YOECandidates need 4-6 years of clinical drug development experience with study start-up, vendor management, and knowledge of ICH/GCP. Strong leadership, negotiation, data-driven planning and proficiency with CTMS, TMF and Microsoft Office are required.

  CTMS, TMF

  1mo

  Senior Clinical Research Associate - FSP

  Quebec +2

  Remote

  PI

  Parexel International (Canada) LTD

  3+ YOECandidates need at least 3 years of clinical research site monitoring experience, extensive knowledge of ICH/GCP, FDA and local regulations, and a life sciences bachelor's or professional degree. They must be fluent in English and the local language, able to travel 60-80%, and hold a valid driver's licence and passport.

  Trial Master File (TMF)

• 1mo

  Associé(e) de recherche clinique (ARC) principal(e) / Senior Clinical Research Associate, Sponsor Dedicated

  Montréal, QC +1

  Full Time

  CC

  CAN Canada

  3+ YOEAu moins 3 ans d'expérience en surveillance sur site; Connaissance approfondie des BPC et de l'ICH; Baccalauréat scientifique ou en soins de santé privilégié

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint, laptop computer, iPhone, iPad

  1mo

  Clinical Research Associate (Canada)

  Kirkland, QC

  Full Time

  CC

  CAN Canada

  Baccalauréat scientifique ou en soins de santé préféré; Connaissance des BPC et des lignes directrices ICH; Maîtrise de Microsoft Word, Excel et PowerPoint

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint, laptop, iPad, iPhone

• 1mo

  Senior Manager/Associate Director, Quality Control

  Burnaby, BC

  $114k–$179k/yrHybridFull Time

  

  Xenon Pharmaceuticals: Xenon Pharmaceuticals is a neuroscience-focused biopharmaceutical company dedicated to drug discovery, clinical development, and commercialization…

  5+ YOE5+ MgmtXenon Pharmaceuticals requires an undergraduate life sciences degree and 5+ years (Senior Manager) or 8+ years (Associate Director) of pharmaceutical management experience. Candidates need strong knowledge of QC testing, ICH stability, OOS/OOT investigations, batch release and quality systems.

  Quality control, Statistical process control, Collaboration, Workflow, CTAS, Quality assurance

5 companies